F(ab)2 Anti-Goat IgG (H&L) (Phycoerythrin Conjugated) Secondary Antibody, Rabbit Polyclonal, R-Phycoerythrin (RPE) validated in IF, FC (ASR2862), Abgent

Phycoerythrin偶联Integrin beta 3抗体[VIPL2](ab91128)可与人样本反应并经Flow Cyt实验严格验证，实验条件参看说明书。Abcam对所有产品均提供质保服务，中国75%以上现货。

Mouse Anti-Human Lymphotoxin beta R Monoclonal Antibody, Phycoerythrin Conjugated, Clone 71319 from R&D Systems,Human LT beta R/TNFRSF3 Phycoerythrin MAb (Clone 71319),biological,biology supply,biology supplies,biology product

Phycoerythrin偶联CD244抗体[244F4](ab95807)可与小鼠样本反应并经Flow Cyt实验严格验证，实验条件参看说明书。Abcam对所有产品均提供质保服务，中国75%以上现货。

Anti-MouseCD120αR-phycoerythrin(R-PE)(TNFR1)MonoclonalAntibodyProd.No.:T247Clone:55R-286Isotype:ArmenianHamsterIgGConc.:0.1mg/mlPkg.Size:50ug,500ugAnti-MouseCD120αR-phycoerythrin(R-PE)(TNF

Pseudanabaena species are poorly known filamentous bloom-forming cyanobacteria closely related to Limnothrix. We isolated 28 Pseudanabaena strains from the Baltic Sea (BS) and the Albufera de Valencia (AV; Spain). By combining phenotypic and genotypic approaches, the phylogeny, diversity and evolutionary diversification of these isolates were explored. Analysis of the in vivo absorption spectra of the Pseudanabaena strains revealed two coexisting pigmentation phenotypes: (i) phycocyanin-rich (PC-rich) strains and (ii) strains containing both PC and phycoerythrin (PE). Strains of the latter phenotype were all capable of complementary chromatic adaptation (CCA). About 65 kb of the Pseudanabaena genomes were sequenced through a multilocus sequencing approach including the sequencing of the16 and 23S rRNA genes, the ribosomal intergenic spacer (IGS), internal transcribed spacer 1 (ITS-1), the cpcBA operon encoding PC and the IGS between cpcA and cpcB. In addition, the presence of nifH, one of the ...

mouse, anti-histidine, igg, mouse anti-6x Histidine, SureLight R-Phycoerythrin, AS15 2931, anti-6x Histidine, conjugated to SureLight R-Phycoerythrin

BioAssay record AID 159272 submitted by ChEMBL: Percent inhibition of 2,2-azobis(2-amidinopropane)dihydrochloride induced decay of (R)-phycoerythrin fluorescence emission.

Abcam provides specific protocols for Anti-CD48 antibody [MEM-102], prediluted (Phycoerythrin) (ab119873) : Flow cytometry protocols

Anti-PDGF Receptor alpha antibody [APA5] (Phycoerythrin) (ab93531) has been cited in 3 publications. References for Mouse in ICC/IF, IHC-Fr, IHC-P

国内在庫あります！Phycoerythrin標識済みマウス・モノクローナル抗体 ab104950 交差種: Ms,Hu,Chmp 適用: Flow Cyt…ROR gamma抗体一覧…

国内在庫あります！Phycoerythrin標識済みマウス・モノクローナル抗体 ab23901 交差種: Hu 適用: Flow Cyt…HLA DR + DP + DQ抗体一覧…

Buy cpeA recombinant protein, B-phycoerythrin alpha chain (cpeA) Recombinant Protein-Q02036.1 (MBS1133381) product datasheet at MyBioSource, Recombinant Proteins

Fremyella diplosiphon CpeR protein: shows similarities to PP2C phosphatases but lacks some residues normally found in PP2C phosphatase catalytic sites; isolated from Fremyella diplosiphon; amino acid sequence in first source

TY - JOUR. T1 - Ambulatory 24-hour double-probe ph monitoring; the importance of manometry. AU - Johnson, Paul E.. AU - Koufman, James A.. AU - Nowak, Lisa J.. AU - Belafsky, Peter C.. AU - Postma, Gregory N.. PY - 2001/11. Y1 - 2001/11. N2 - Objective Historically, manometry has been used for sphincter localization before ambulatory 24-hour double-probe pH monitoring to ensure accurate placement of the probes. Recently, direct-vision placement (DVP), using transnasal fiberoptic laryngoscopy (TFL), has been offered as an alternative technique. Presumably, DVP might be used to precisely place the proximal (pharyngeal) pH probe; however, using DVP, there appears to be no way to accurately position the distal (esophageal) probe. The purpose of this study was to evaluate the accuracy of DVP for pH probe placement using manometric measurement as the gold standard. Methods Thirty patients undergoing pH monitoring participated in this prospective study. Each subject underwent manometric examination of ...

Fluodyn B-Phycoerythrin labeling from Biosciencia laboratory is perfect to create bioconjugates with antibody and protein labeling. BPE fluorescent dye is incredibly bright and allows hignher sensibility and less background.

Plays a role in phycoerythrobilin biosynthesis, the red pigment chromophore photosynthetically active biliproteins of the host cyanobacteria. Uses a four-electron reduction to carry out the reactions catalyzed by two enzymes (EC 1.3.7.2 and EC 1.3.7.3) in host.

Synechococcus cpeA protein: a class I Phycoerythrin (PE) alpha subunit gene product; from cyanobacterium, Synechococcus; amino acid sequence given in first source; GenBank X72961; do not confuse with cpeA gene product, Rhodobacter, a catalase-peroxidase

Special note about Community Feature Content. Any content and/or opinions uploaded, expressed or submitted through any Community Feature or any other publicly available section of the Web Site (including password-protected areas), and all articles and responses to questions, other than the content explicitly authorized by the Company, are solely the opinions and responsibility of the person or entity submitting them and do not necessarily reflect the opinions of the Company. By way of example, any recommended or suggested use of products or services available from the Company that is posted through a Community Feature is not a sign of approval or recommendation by the Company. If you choose to follow any such recommendation you do so at your own risk.. Links to Third Party Sites. The Web Site may contain links to other websites on the internet. The Company is not responsible for the content, products, services or practices of any third party websites, including without limitation sites linked to ...

Special note about Community Feature Content. Any content and/or opinions uploaded, expressed or submitted through any Community Feature or any other publicly available section of the Web Site (including password-protected areas), and all articles and responses to questions, other than the content explicitly authorized by the Company, are solely the opinions and responsibility of the person or entity submitting them and do not necessarily reflect the opinions of the Company. By way of example, any recommended or suggested use of products or services available from the Company that is posted through a Community Feature is not a sign of approval or recommendation by the Company. If you choose to follow any such recommendation you do so at your own risk.. Links to Third Party Sites. The Web Site may contain links to other websites on the internet. The Company is not responsible for the content, products, services or practices of any third party websites, including without limitation sites linked to ...

Author(s): Chen, Z; Kaplan, DL; Yang, K; Kumar, J; Marx, KA; Tripathy, SK | Abstract: Light transducing phycobiliproteins are encapsulated in optically transparent sol-gel matrices. Absorption and fluorescence spectroscopies are used to characterize the effect of the sol-gel encapsulation on the conformation and aggregation states of the three major phycobiliproteins present in phycobilisomes: phycoerythrin, phycocyanin, and allophycocyanin. It is found that the effects of sol-gel entrapment on the spectroscopic properties are significantly different for the three phycobiliproteins. The results indicate that phycoerythrin undergoes only minor change in its native structure when entrapped in sol-gel. However, significant changes in conformation and aggregation state occur when phycocyanin and allophycocyanin are entrapped in sol-gel matrices. A thin film of sol-gel encapsulated phycoerythrin is also coated on an optical fiber surface and strong fluorescence from the evanescent wave excitation is detected

TY - JOUR. T1 - Excitation dynamics in phycoerythrin 545. T2 - Modeling of steady-state spectra and transient absorption with modified redfield theory. AU - Novoderezhkin, Vladimir I.. AU - Doust, Alexander B.. AU - Curutchet, Carles. AU - Scholes, Gregory D.. AU - Van Grondelle, Rienk. PY - 2010/7/21. Y1 - 2010/7/21. N2 - We model the spectra and excitation dynamics in the phycobiliprotein antenna complex PE545 isolated from the unicellular photosynthetic cryptophyte algae Rhodomonas CS24. The excitonic couplings between the eight bilins are calculated using the CIS/6-31G method. The site energies are extracted from a simultaneous fit of the absorption, circular dichroism, fluorescence, and excitation anisotropy spectra together with the transient absorption kinetics using the modified Redfield approach. Quantitative fit of the data enables us to assign the eight exciton components of the spectra and build up the energy transfer picture including pathways and timescales of energy relaxation, ...

Mouse/Rat Anti-Canine CD3 / CD4 Dual Colour Reagent Antibody, FITC / R-Phycoerythrin Conjugated from AbD Serotec,MSE ANTI CAN. CD3:FITC/RAT ANTI CD4:RPE,biological,biology supply,biology supplies,biology product

Synechococcus is a cosmopolitan genus of picocyanobacteria living in the photic zone of freshwater and marine ecosystems. Here, we describe the isolation of 46 closely related picocyanobacterial strains from the Baltic Sea. The isolates showed considerable variation in their cell size and pigmentation phenotypes, yielding a colorful variety of red, pink and blue-green strains. These pigmentation phenotypes could not be differentiated on the basis of their 16S rRNA-internal transcribed spacer (ITS) sequences. Thirty-nine strains, designated BSea, possessed 16S rRNA-ITS sequences almost identical with Synechococcus strain WH5701. Despite their similar 16S rRNA-ITS sequences, the BSea strains separated into several different clusters when comparing the phycocyanin (cpcBA) operon. This separation was largely consistent with the phycobiliprotein composition of the different BSea strains. The majority of phycocyanin (PC)-rich Bsea strains clustered with WH5701. Remarkably, the phycoerythrin (PE)-rich ...

Four-color flow cytometry was performed on freshly isolated PBMCs, to investigate the cell surface expression of CD14, CD16, TLR-2, and TLR-4, on monocytes of patients with ED and healthy controls. Briefly, PBMCs were washed twice with phosphate-buffered saline (PBS; 0.02 M, pH 7.2) and resuspended in PBS containing 2% heat-inactivated fetal bovine serum (FBS). Fifty microliters of PBMC suspension (1 × 106 cells/mL) was incubated with primary antibodies for 30 minutes at room temperature: fluorescein isothiocyanate (FITC)-conjugated anti-CD14 (clone 61D3, eBioscience, San Diego, CA), phycoerythrin cyanine 5 (PECy5)-conjugated anti-CD16 (clone 3G8, BioLegend, San Diego, CA), allophycocycanin (APC)-conjugated anti-TLR-2 (clone TL2.1; eBioscience), and phycoerythrin (PE)-conjugated anti-TLR-4 (clone HTA125, eBioscience), along with isotype-matched antibody controls. After they were washed with PBS, the cells were resuspended in 400 μL PBS containing 2% FBS, and counts were acquired on a ...

Red blood cells were lysed by adding lysis buffer (distilled water containing 0.15 m ammonium chloride, 0.01 m potassium bicarbonate and 0.08 mm tetrasodium EDTA, pre-warmed to 37°C) to 500 μL EDTA-treated whole blood, mixing continuously for 5 min. Cells were washed twice and reconstituted in 500 μL flow buffer [1% bovine serum albumin (BSA)/phosphate-buffered saline (PBS)]. Monoclonal antibodies directed against CD4, CD8 or CD28 (Immunotech, Marseilles, France) conjugated with fluorescein isothiocyanate (FITC), phycoerythrin (PE) or phycoerythrin cyanin 5.1 (PCy5) and 50 μL cells were added to flow tubes. Tubes were vortexed and incubated for 15 min at room temperature. A volume of 100 μL IntraPrep Permeabilization Reagent 1 (Immunotech) was then added and tubes were vortexed and incubated for 15 min at room temperature.. Cells were washed in flow buffer and 100 μL IntraPrep Permeabilization Reagent 2 was added without mixing. Tubes were incubated for 5 min at room temperature, then ...

This dataset includes photosynthetic pigment concentrations in Plocamium cartilagineum grown under various temperatures and CO2 levels, from July 2014 to February 2015. The parameters reported are: the concentrations of Chlorophyll a, Phycoerythrin, Phycocyanin, Allophycocyanin, and total Phycobiliprotein, and the ratio of total Phycobiliprotein to Chlorophyll A. For a complete list of measurements, refer to the full dataset description in the supplemental file Dataset_description.pdf. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/ ...

ID PROMP_1_PE100 STANDARD; PRT; 555 AA. AC PROMP_1_PE100; Q7V3H5; DT 00-JAN-0000 (Rel. 1, Created) DT 00-JAN-0000 (Rel. 2, Last sequence update) DT 00-JAN-0000 (Rel. 3, Last annotation update) DE SubName: Full=L-aspartate oxidase; EC=1.4.3 16; (PROMP_1.PE100). GN Name=nadB; OrderedLocusNames=PMM0100; OS PROCHLOROCOCCUS MARINUS SUBSP. PASTORIS STR. CCMP1986. OC Bacteria; Cyanobacteria; Prochlorales; Prochlorococcaceae; OC Prochlorococcus. OX NCBI_TaxID=59919; RN [0] RP -.; RG -.; RL -.; CC -!- SEQ. DATA ORIGIN: Translated from the HOGENOM CDS PROMP_1.PE100. CC Prochlorococcus marinus subsp. pastoris str. CCMP1986, complete genome. CC genome. CC -!- ANNOTATIONS ORIGIN:Q7V3H5_PROMP CC -!- GENE_FAMILY: HOG000160476 [ FAMILY / ALN / TREE ] DR UniProtKB/Swiss-Prot; Q7V3H5; -. DR EMBL; BX548174; CAE18559.1; -; Genomic_DNA. DR RefSeq; NP_892221.1; NC_005072.1. DR HSSP; P83223; 1D4D. DR ProteinModelPortal; Q7V3H5; -. DR STRING; Q7V3H5; -. DR GeneID; 1725749; -. DR GenomeReviews; BX548174_GR; PMM0100. DR ...

Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More... ...

On July 1, 2021, Dr. Evan Glazer will become IMSAs fifth president. He will succeed President Dr. Jose M. Torres and current Interim President Dr. Norman Storm Robinson III. As IMSA enters a crucial phase in its history over the next few months, Dr. Glazer must balance a variety of responsibilities in his new role. The Acronyms Oliver Ni and Liz Alcala interviewed Dr. Glazer to learn about his STEM background, his goals for his new position, and what he hopes the future of IMSA will look like.. While this will be his first time working at IMSA, Dr. Glazer has had a long history of interacting with our school. During his time working at Thomas Jefferson High School for Science and Technology, Dr. Glazer became acquainted with various members of IMSA staff and administration. According to Dr. Glazer, teachers at IMSA would go to similar conferences as teachers at TJ. Ive gotten to know [Dr. Glenn] Max McGee in particular, who was a former president when I was at TJ. Dr. Glazer saw multiple ...

Fig. 3. Isolation and characterization of N332-dependent antibodies isolated using native-like SOSIP trimers and synthetic Man9-V3 glycopeptide.. (A) ELISA binding analyses of plasma from the HIV-infected donor CH765 to Man9-V3 and aglycone V3 peptides. Donor plasma was screened in duplicate assays, and binding is represented as mean values. (B) Memory B cells from donor CH765 were decorated with either fluorophore-conjugated BG505.T332N.SOSIP and DU156.12.SOSIP in phycoerythrin (PE) and allophycocyanin (APC), or Man9-V3 tetramers tagged to SA-AF647 (Alexa Fluor 647) and SA-BV421 (Brilliant Violet 421). The B cells from which CH765-VRC41.01, VRC41.02, and DH563 were cloned are indicated as green, red, and blue dots, respectively. (C) Immunogenetics and phylogeny of the DH563-VRC41 clonal lineage were inferred using Clonanalyst (33, 34). See also fig. S3. nt, nucleotide. (D) Reactivity of CH765-VRC41.01, CH765-VRC41.02, and DH563 to Man5, Man6, Man7-D1, Man7-D3, Man8-D1D3, and Man9 glycans, ...

C3/C6P solid secondary standard insert (for chlorophyll, rhodamine, fluorescein, phycoerythrin and phycocyanin only), requires cap

We have applied quantum dot (Qdot) antibody conjugates as a biomolecular probe for cellular proteins important in biogeochemical cycling in the sea. Conventional immunological methods have been hampered by the strong autofluorescence found in cyanobacteria cells. Qdot conjugates provide an ideal alternative for studies that require long-term imaging of cells such as detection of low abundance cellular antigens by fluorescence microscopy. The advantage of Qdot labeled probes over conventional immunological methods is the photostability of the probe. Phycoerythrin bleaches in cyanobacterial cells under prolonged UV or blue light excitation, which means that the semiconducting nanocrystal probe, the Qdot, can yield a strong fluorescent signal without interference from cellular pigments.

The advantage of 7-AAD over PI is the ability to be used in conjunction with phycoerythrin (PE)- and fluorescein isothiocyanate (FITC)-labeled monoclonal antibodies in 2-color analysis, with minimal spectral overlap between 7-AAD, PE and FITC fluorescence emissions. The 7-AAD fluorescence is detected in the far red range of the spectrum (650 nm long-pass filter ...

CELI : LABType applies Luminex technology to the reverse sequence-specific oligonucleotide (SSO) DNA typing method. First, target DNA is PCR-amplified using a group-specific primer. The PCR product is biotinylated, which allows it to be detected using R-phycoerythrin-conjugated streptavidin. The PCR product is denatured and allowed to rehybridize to complementary DNA probes conjugated to fluorescently coded microspheres. A flow analyzer identifies the fluorescent intensity of phycoerythrin on each microsphere. The HLA Class II allele or allele groups of the sample is determined by the positive and negative bead IDs using a computer software program. The assignment of the HLA typing is based on the reaction pattern compared to patterns associated with published HLA gene sequences.(Package insert: One Lambda, LABType SSO Typing)

The Gal1,3GalNAc1,O-Ser/Thr particular lectin from (improved cell proliferation just like those cells activated via CD3/CD28 at 48?h of tradition. well mainly because soluble and intracellular cytokines, as well as the incomplete characterization of the primary lipid raft glycoprotein identified by seed products were acquired in Tulyehualco (Mexico) as well as the lectin was purified simply by affinity chromatography mainly because referred to previously 9. was tagged using the N-hydroxysuccinimide ester of biotin from Pierce Chemical substance (Rockford, IL) having a label/proteins percentage of 2:1 16. Phycoerythrin (PE)-tagged rat anti-mouse Compact disc4, biotin-labeled hamster anti-mouse Compact disc3? string YK 4-279 (145-2C11) monoclonal antibodies (mAbs), and PE-labeled rat IgG2a, kappa mAb (utilized as isotype control); purified no azide/low endotoxin (NA/LE) hamster anti-CD3 (clone 145-2C11) or anti-CD28 (clone 37.51) mAbs (utilized to activate T cells); PE-cyanine (Cy) 5-, fluorescein ...

The Gal1,3GalNAc1,O-Ser/Thr particular lectin from (improved cell proliferation just like those cells activated via CD3/CD28 at 48?h of tradition. well mainly because soluble and intracellular cytokines, as well as the incomplete characterization of the primary lipid raft glycoprotein identified by seed products were acquired in Tulyehualco (Mexico) as well as the lectin was purified simply by affinity chromatography mainly because referred to previously 9. was tagged using the N-hydroxysuccinimide ester of biotin from Pierce Chemical substance (Rockford, IL) having a label/proteins percentage of 2:1 16. Phycoerythrin (PE)-tagged rat anti-mouse Compact disc4, biotin-labeled hamster anti-mouse Compact disc3? string YK 4-279 (145-2C11) monoclonal antibodies (mAbs), and PE-labeled rat IgG2a, kappa mAb (utilized as isotype control); purified no azide/low endotoxin (NA/LE) hamster anti-CD3 (clone 145-2C11) or anti-CD28 (clone 37.51) mAbs (utilized to activate T cells); PE-cyanine (Cy) 5-, fluorescein ...

Start with as little or as much as you want. Businesses or individuals can enroll in Green Lights to match a small portion of overall energy use, or offset all the way up to 100 percent. Theres no time commitment and you can choose to stop monthly Green Lights participation at any time.. You choose the number of 100 kilowatt-hour blocks of Green Lights you wish to buy. One block of Green Lights is $1 per month. To offset the total energy use of an average home is about $15, equal to 1500 kWh. If your businesss monthly electricity use is 10,000 kWh, participating in Green Lights at 10% is only $10. ...

Chicken IgG (H+L), 0.2 ml. Immunoglobulin G (IgG), is one of the most abundant proteins in serum with normal levels between 8-17 mg/mL in adult blood.

Pig IgG (H+L), 0.2 ml. Immunoglobulin G (IgG), is one of the most abundant proteins in serum with normal levels between 8-17 mg/mL in adult blood.

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dlls/shell32/tests/ebrowser.c , 84 +++++++++++++++++++++++++++++++++++++++++ 1 files changed, 84 insertions(+), 0 deletions(-) diff --git a/dlls/shell32/tests/ebrowser.c b/dlls/shell32/tests/ebrowser.c index d8f1677..8fa8b9a 100644 --- a/dlls/shell32/tests/ebrowser.c +++ b/dlls/shell32/tests/ebrowser.c @@ -56,6 +56,13 @@ static HRESULT ebrowser_initialize(IExplorerBrowser *peb) return IExplorerBrowser_Initialize(peb, hwnd, &rc, NULL); } +static HRESULT ebrowser_browse_to_desktop(IExplorerBrowser *peb) +{ + LPITEMIDLIST pidl_desktop; + SHGetSpecialFolderLocation (hwnd, CSIDL_DESKTOP, &pidl_desktop); + return IExplorerBrowser_BrowseToIDList(peb, pidl_desktop, 0); +} + /* Process some messages */ static void process_msgs(void) { @@ -316,6 +323,26 @@ static void test_SB_misc(void) IShellBrowser_Release(psb); IExplorerBrowser_Destroy(peb); + IExplorerBrowser_Release(peb); + + /* Browse to the desktop. */ + ebrowser_instantiate(&peb); + ebrowser_initialize(peb); + IExplorerBrowser_QueryInterface(peb, ...

Jch 120 5 Roll Case BlackHelp keep your film protected and organized with this black Film Hard Case from Japan Camera Hunter, which holds 5 rolls o.... View full details ...

Porphyridium cruentum is a species of red alga in the family Porphyridiophyceae.. The microalga Porphyridium sp. is a potential source for several products like fatty acids, lipids, cell-wall polysaccharides and pigments . The polysaccharides of this species are sulphated and their structure gives rise to some unique properties that could lead to a broad range of industrial and pharmaceutical applications. Additionally, P. cruentum biomass contains carbohydrates of up to 57% have been reported. Thus, the combined amount of carbohydrates in biomass and exopolysaccharides of this microalga could potentially provide the source for bio-fuel and pharmaceutical [1][2]. The genus Porphyridium has been classified among blue-green, red, and green algae.[3]. ...

An electron microscopic examination of Porphyridium cruentum revealed the presence of mitochondria which had been reported absent in this aerobic organism. The chloroplast in this red alga was found to contain small granules (about 320 A) regularly arranged along the parallel chloroplast lamellae. The chloroplast granules differ in size and staining intensity from the ribosomes located in the cytoplasm. Two tubular elements are described. One type (450 to 550 A) is associated with the Golgi bodies. Another type (350 A), in the cell periphery, is believed to connect the endoplasmic reticulum and the cell membrane. Daughter nuclei were found to be positioned at opposite ends of the cell prior to commencement of cell division. Cytokinesis is accomplished by an annular median constriction causing the gradual separation of the chloroplast, pyrenoid, and other cell organelles, resulting in two equal daughter cells. No appreciable differences were observed between cells grown in high light (400 ft-c) ...

The chlorophyll-binding subunits of photosystems I and II are internal antenna light-harvesting proteins of oxygenic photosynthesis. The antenna proteins that exist in phycobilisomes in cyanobacteria and light-harvesting chlorophyll protein complexes in green plants act as peripheral antenna systems, enabling more efficient absorption of light energy ...

The Rhodophyta (red algae) are a distinct eukaryotic lineage characterized by the accessory photosynthetic pigments phycoerythrin, phycocyanin and allophycocyanins arranged in phycobilisomes, and the absence of flagella and centrioles (Woelkerling 1990). This is a large assemblage of between 2500 and 6000 species in about 670 largely marine genera (Woelkerling 1990) that predominate along the coastal and continental shelf areas of tropical, temperate and cold-water regions (L ning 1990). Red algae are ecologically significant as primary producers, providers of structural habitat for other marine organisms, and their important role in the primary establishment and maintenance of coral reefs. Some red algae are economically important as providers of food and gels. For this reason, extensive farming and natural harvest of red algae occurs in numerous areas of the world.. ...

The Rhodophyta (red algae) are a distinct eukaryotic lineage characterized by the accessory photosynthetic pigments phycoerythrin, phycocyanin and allophycocyanins arranged in phycobilisomes, and the absence of flagella and centrioles (Woelkerling 1990). This is a large assemblage of between 2500 and 6000 species in about 670 largely marine genera (Woelkerling 1990) that predominate along the coastal and continental shelf areas of tropical, temperate and cold-water regions (L ning 1990). Red algae are ecologically significant as primary producers, providers of structural habitat for other marine organisms, and their important role in the primary establishment and maintenance of coral reefs. Some red algae are economically important as providers of food and gels. For this reason, extensive farming and natural harvest of red algae occurs in numerous areas of the world.. ...

p>The checksum is a form of redundancy check that is calculated from the sequence. It is useful for tracking sequence updates.,/p> ,p>It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low.,/p> ,p>However UniProtKB may contain entries with identical sequences in case of multiple genes (paralogs).,/p> ,p>The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x,sup>64,/sup> + x,sup>4,/sup> + x,sup>3,/sup> + x + 1. The algorithm is described in the ISO 3309 standard. ,/p> ,p class=publication>Press W.H., Flannery B.P., Teukolsky S.A. and Vetterling W.T.,br /> ,strong>Cyclic redundancy and other checksums,/strong>,br /> ,a href=http://www.nrbook.com/b/bookcpdf.php>Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993),/a>),/p> Checksum:i ...

A strain of the filamentous non N-fixing cyanobacterium Phormidium sp. isolated from the Messolonghi (W. Greece) saltworks, was cultured in the laboratory at 6 different combinations of salinity (20-40-60 ppt) and illumination (low-2000 lux and high-8000 lux). At salinities of 60 and 40 ppt and in high illumination (XL-8000 lux) the growth rate (μmax) presented the highest values (0.491 and 0.401 respectively) compared to the corresponding at 20 ppt (0.203). In general and at all salinities, the higher illumination (XL) gave the highest growth rates and shorter dublication time (tg) in comparison to the lower illumination (L). On the contrary, phycocyanin, phycoerythrin and allophycocyanin production was extremely increased in the lower illumination (L) in all salinities, from ~14fold at 40 and 60 ppt to 269fold at 20 ppt of those corresponding to higher illumination (XL). Similar analogies were also recorded for the other two billiproteins. Chlorophyll-a content was also higher in lower illumination

Dr Sanjiv Kumar Mishra is CEO and founder member of Algallio Biotech Private Limited, He worked as Post-Doctoral researcher in the area of microalgal technology for value-added products like Phycocyanin, Phycoerythrin, DHA and downstream processing for fuel production, at Advanced Biomass R&D Center, KAIST; Republic of Korea. After receiving his PhD in 2012 in Microbiology from the (CSIR-CSMCRI) Bhavnagar University, Dr Sanjiv began his professional scientific career as post-doc by joining the research Group of Prof. Ji-Won Yang in KAIST to study microalgal biofuel, microalgal bacterial interaction, cyanobacteria biotechnology, fluorescent proteins, microalgal harvesting and extraction . He has also been awarded DAAD fellowship to carry out research in ICBM, Oldenburg, Germany. His major research interest is to develop technology to produce microalgal-based biofuels and valuable natural products that can be economically sustainable. His 11 years of research experience cover various fields of ...

Fluorescence is used in the life sciences generally as a non-destructive way of tracking or analysing biological molecules by means of fluorescence. Some proteins or small molecules in cells are naturally fluorescent, which is called intrinsic fluorescence or autofluorescence (such as NADH, tryptophan or endogenous Chlorophyll, Phycoerythrin or green fluorescent protein). Alternatively, specific or general proteins, nucleic acids, lipids or small molecules can be labelled with an extrinsic fluorophore, a fluorescent dye which can be a small molecule, protein or quantum dot. Several techniques exist to exploit additional properties of fluorophores, such as fluorescence resonance energy transfer, where the energy is passed non-radiatively to a particular neighbouring dye, allowing proximity or protein activation to be detected; another is the change in properties, such as intensity, of certain dyes depending on their environment allowing their use in structural studies. Play media Play media The ...

Peripheral blood lymphocytes from 9 monoclonal gammopathies of undetermined significance (MGUS) and 27 multiple myelomas (MM) were studied with a panel of monoclonal antibodies (MoAb) that recognize B and T lymphocytes and plasma cells. No difference in the percentage of B lymphocytes, identified by B1 and B4 MoAb, was observed in MGUS and MM patients versus normal controls. However, high percentages of circulating lymphocytes expressing plasma cell-associated antigens were detected in MM (HAN-PC1+ = 29.4 +/- 20.4%; TEC-T10+ = 27.8 +/- 19.2%) whereas they were in the normal range in MGUS (HAN-PC1+ = 8.8 +/- 5.8% p = 0.006; TEC-T10+ = 5.7 +/- 4.7% p less than 0.001). Almost identical results were obtained using PCA-1 MoAb in 17 of these patients. TEC-T10+ and PCA-1+ lymphocytes were sorted and re-analyzed with phycoerythrin conjugated MoAb in 3 healthy subjects, 2 MGUS, and 4 MM patients. In normal subjects and in MGUS the majority of PCA-1+ cells belonged to the B lineage (Leu 2-, Leu3-, Leu ...

Materials. Peridinin chlorophyll protein-labeled anti-HLA-DR, FITC-conjugated anti-CD80, phycoerythrin (PE)-conjugated anti-CD86, PE-conjugated anti-CD40, and FITC-labeled anti-CD8 were purchased from BD Biosciences PharMingen (Chicago, IL). FITC-conjugated anti-HLA-A2 monoclonal antibody (clone BB7.2) was from Serotec Ltd. (Oxford, United Kingdom). Anti-human CEA (CE05) was from Neomarker (Fremont, CA). Anti-HSP27 (F-4), anti-HSP40 (C-20), anti-HSP60 (H-1), anti-HSP70 (K-20), anti-Hsc70 (B6), anti-intercellular adhesion molecule-1 (C-19), anti-B7.1 (N-20), anti-B7.2 (C-19), anti-transferrin receptor (K-20), and anti-lysosome-associated membrane glycoprotein-3 were from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA). Anti-MHC-I (HC10) was from Roswell Park Cancer Institute (Buffalo, NY). Horseradish peroxidase-coupled secondary antibodies were from Jackson ImmunoResearch (West Grove, PA). Recombinant mouse interleukin (IL)-2 and recombinant human IL-2 were commercially obtained from Sigma (St. ...

Chroma Catalog Sets: ET - Cy3/Cy5 | ET Series, FRET 双波段带通 | Included Filters: ET545/25x, ET640/30x, 59007bs, ET595/50m, ET690/50m | Related Fluorochromes: Propidium Iodide, Quasar® 570, DiI, MitoTracker Orange/MeOH, Cy3™, Rhod-2, Alexa Fluor 555™, tdTomato, DyLight 549, Atto 550, TAMRA, Tetramethylrhodamine isothiocyanate, TRITC, Alexa Fluor 546™, TagRFP, DsRed, R-phycoerythrin, CAL Fluor® Red 590, Rhodamine Red™-X, AsRed2, FusionRed, LysoTracker Red/pH 5.2, Alexa Fluor 568™, ROX, MitoTracker Red/MeOH, X-rhod-1/Ca2+, Cy3.5™, TO-PRO™-3, DiD, MitoTracker Deep Red 633/MeOH, Atto 647N, Draq5, Quasar® 670, Alexa Fluor 647™, Cy5™, Allophycocyanin (APC), SYTO® 60, DyLight 649 |

7-AAD Staining Solution is a ready-to-use reagent suitable for the evaluation of cell viability in mono- or multiparametric analyses of human peripheral blood using flow cytometry. 7-AAD (7-amino-actinomycin D) is a fluorescent dye that intercalates into double-stranded DNA (GC rich regions). It is excluded from viable cells, but can penetrate cell membranes of dead or dying cells. Therefore, it can be used instead of propidium iodide (PI) for the evaluation of cell death and apoptosis. The fluorescence emission maximum for 7-AAD is at 647 nm. When excited at 488 nm, 7-AAD is detected in the red fluorescence channel commonly used for R-phycoerythrin (PE)-Cy® 5 tandem dye detection, with minimal spectral overlap into the yellow fluorescence channel commonly used for PE detection. - Schweiz

7-AAD Staining Solution is a ready-to-use reagent suitable for the evaluation of cell viability in mono- or multiparametric analyses of human peripheral blood using flow cytometry.7-AAD (7-amino-actinomycin D) is a fluorescent dye that intercalates into double-stranded DNA (GC rich regions). It is excluded from viable cells, but can penetrate cell membranes of dead or dying cells. Therefore, it can be used instead of propidium iodide (PI) for the evaluation of cell death and apoptosis.The fluorescence emission maximum for 7-AAD is at 647 nm. When excited at 488 nm, 7-AAD is detected in the red fluorescence channel commonly used for R-phycoerythrin (PE)-Cy®5 tandem dye detection, with minimal spectral overlap into the yellow fluorescence channel commonly used for PE detection. - Nederland

This graph shows the total number of publications written about Phycobilisomes by people in this website by year, and whether Phycobilisomes was a major or minor topic of these publications ...

SWISS-MODEL Template Library (SMTL) entry for 2xcz.1. Crystal Structure of macrophage migration inhibitory factor homologue from Prochlorococcus marinus

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[112 Pages Report] Check for Discount on Global Pharmaceutical Grade Phycocyanin Market Professional Survey Report 2017 report by QYResearch Group. This report studies Pharmaceutical Grade Phycocyanin in Global market, especially...

A single cell with a stellate chloroplast. This culture contains sufficient material for a class of 100 students. To be sure you order enough material for your class, please use …

Fluorescent Dyes , Fluorescent Proteins , CL-APC (Cross Linked-Allophycocyanin); Allophycocyanin (APC), highly fluorescent phycobiliprotein, is made up of alpha and beta subunits and is present as a trimer (αβ)3, which is unstable and susceptible to dissociation at low concentrations. The monomer, αβ, has a lower fluorescence quantum yield compared to the trimer and the maximal absorption is also shifted to 620 nm. The chemically cross-linked APC trimer is much more stable than the native APC trimer, but still retains the same spectroscopic properties as the native APC trimer. APC labeled streptavidin, primary and secondary antibodies have been widely used in applications such as flow cytometry, live cell staining, and immunofluorescent staining.

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It has long been flagged as the future for food, and now a WA start-up company has been given the green light to sell crickets for human consumption.

Spains footballing authorities have given Barcelona the green light to make an emergency signing after confirming forward Ousmane Dembele will miss at least the next six months with a hamstring issue.

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The atheist bus adverts that declare theres probably no God have been given the green light by the advertising watchdog, despite attracting hundreds of complaints.

APs founder appeared on Dr. Oz where he shared his expertise on how fake news and ad fraud is being used in the performance marketing space.

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Well, it seems that you, the web video watching public, has spoken. Amazon announced today that it has whittled its robust list of pilots down to five titles,...

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Green light given for a Dwight centered spinoff. Im excited because I absolutely love Dwight. Looking forward to see what that crazy German does. http://www.comingsoon.net/news/tvnews.php?id=93739